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van Rijn, R. M.

Publications and source records attributed to van Rijn, R. M..

2 recordsLinked to original sources

Rubsicolins are naturally occurring G-protein-biased delta opioid receptor peptides

The impact that {beta}-arrestin proteins have on G-protein-coupled receptor trafficking, signaling and physiological behavior has gained much appreciation over the past decade. A number of studies have attributed the side effects associated with the use of naturally occurring and synthetic opioids, such as respiratory depression and constipation, to excessive recruitment of {beta}-arrestin. These findings have led to the development of biased opioid small molecule agonists that do not recruit {beta}-arrestin, activating only the canonical G-protein pathway. Similar G-protein biased small molecule opioids have been found to occur in nature, particularly within kratom, and opioids within salvia have served as a template for the synthesis of other G-protein-biased opioids. Here, we present the first report of naturally occurring peptides that selectively activate G-protein signaling pathways with minimal {beta}-arrestin recruitment. We find that rubiscolin peptides, which are produced as cleavage products of the plant protein rubisco, bind to and activate G-protein signaling at {delta} opioid receptors. However, unlike the naturally occurring {delta} opioid peptides leu-enkephalin and deltorphin II, the rubiscolin peptides only very weakly recruit {beta}-arrestin 2 and have undectable recruitment of {beta}-arrestin 1 at the {delta} opioid receptor.

pharmacology and toxicology

Functional histamine H3 and adenosine A2A receptor heteromers in recombinant cells and rat striatum

In the striatum, histamine H3 receptors (H3Rs) are co-expressed with adenosine A2A receptors (A2ARs) in the cortico-striatal glutamatergic afferents and the GABAergic medium-sized spiny neurons that originate the indirect pathway of the basal ganglia. This location allows H3Rs and A2ARs to regulate the striatal GABAergic and glutamatergic transmission. However, whether these receptors interact to modulate the intra-striatal synaptic transmission has not yet been assessed. To test this hypothesis a heteromer-selective in vitro assay was used to detect functional complementation between a chimeric A2AR302-Gqi4 and wild-type H3Rs in transfected HEK-293 cells. H3R activation with the agonist RAMH resulted in Ca2+ mobilization (pEC50 7.31 {+/-} 0.23; maximal stimulation, Emax 449 {+/-} 25 % of basal) indicative of receptor heterodimerization. This response was not observed with histamine, suggesting a RAMH bias for heteromers. Functional A2AR-H3R heteromers were confirmed by co-immunoprecipitation and observations of differential cAMP signaling when both receptors were co-expressed in the same cell. In membranes from rat striatal synaptosomes, H3R activation decreased A2AR affinity for the agonist CGS-21680 (pKi values 8.10 {+/-} 0.04 and 7.70 {+/-} 0.04). Moreover, H3Rs and A2ARs co-immunoprecipitated in protein extracts from striatal synaptosomes. These results support the existence of a H3R/A2AR heteromer, and reveal a new mechanism by which these receptors may modulate the unction of the striatum and the basal ganglia.

neuroscience